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What causes autoimmune disease?
What causes autoimmune disease? Answered by Nat Jones RPH, FAPC https://youtu.be/WchiLv9c9-Y For information on LDN, go to https://linktr.ee/ldnrt Our webinars and training courses can be purchased from https://www.ldnrtevents.com/collections/webinars-and-training-courses We have a list of
What causes autoimmune disease? Answered by Nat Jones RPH, FAPC https://youtu.be/WchiLv9c9-Y For information on LDN, go to https://linktr.ee/ldnrt Our webinars and training courses can be purchased from https://www.ldnrtevents.com/collections/webinars-and-training-courses We have a list of
Shewulf
Administrator
in
LDN Research Trust
1 day ago
Intermittent Fasting Shows Promise in Multiple Sclerosis
Intermittent fasting -- defined as restricting food and drink to 500 calories a day, twice a week -- was safe and successful in a small randomized trial of patients with relapsing-remitting multiple sclerosis (MS).
[u]
Key Takeaways
[/u]
Intermittent calorie restriction lowered leptin
Intermittent fasting -- defined as restricting food and drink to 500 calories a day, twice a week -- was safe and successful in a small randomized trial of patients with relapsing-remitting multiple sclerosis (MS).
[u]
Key Takeaways
[/u]
Intermittent calorie restriction lowered leptin
BettysMom
in
My MSAA Community
2 days ago
Given Private Diagnosis But Antibody Test Is Negative? A Little Confused.
I recently had a private diagnosis of Autoimmune Thyroiditis. This was given in the context of seeking a diagnosis of my B12 deficiency which was said to be linked with the above, Pernicious Anaemia, antibodies attacking thyroid and gastric parietal cells. I have been on levothyroxin for 15yrs. He based
I recently had a private diagnosis of Autoimmune Thyroiditis. This was given in the context of seeking a diagnosis of my B12 deficiency which was said to be linked with the above, Pernicious Anaemia, antibodies attacking thyroid and gastric parietal cells. I have been on levothyroxin for 15yrs. He based
B12again
in
Pernicious Anaemia Society
2 days ago
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Here's the tee shirt I'd like to see!
Multiple Sclerosis - "It's the stuff God hits your ass with when he doesn't want to kill ya -- just slow ya down." Richard Pyror, 1993, [i]Entertainment Weekly[/i]
Multiple Sclerosis - "It's the stuff God hits your ass with when he doesn't want to kill ya -- just slow ya down." Richard Pyror, 1993, [i]Entertainment Weekly[/i]
goatgal
in
My MSAA Community
2 days ago
Given Private Diagnosis But Antibody Test Is Negative?
I recently had a private diagnosis of Autoimmune Thyroiditis. This was given in the context of seeking a diagnosis of my B12 deficiency which was said to be linked with the above, Pernicious Anaemia, antibodies attacking thyroid and gastric parietal cells. I have been on levothyroxin for 15yrs. He based
I recently had a private diagnosis of Autoimmune Thyroiditis. This was given in the context of seeking a diagnosis of my B12 deficiency which was said to be linked with the above, Pernicious Anaemia, antibodies attacking thyroid and gastric parietal cells. I have been on levothyroxin for 15yrs. He based
B12again
in
Thyroid UK
2 days ago
Using regain with under active thyroid.
Hi everybody. I used regain years ago before I was diagnosed with underactive thyroid, I must have been loosing my hair due to my thyroid. The side effects were awful, I would wake up with heart palpitations in the middle of the night. I'm just wondering now that my thyroid is functioning better with
Hi everybody. I used regain years ago before I was diagnosed with underactive thyroid, I must have been loosing my hair due to my thyroid. The side effects were awful, I would wake up with heart palpitations in the middle of the night. I'm just wondering now that my thyroid is functioning better with
MrTHG
in
Thyroid UK
5 days ago
Still fighting for a diagnosis B12, PA
Due to my ongoing failing health I've had to do my own research as to the pathway of blood test results, symptoms and the progression/knock on effects of having doctors who refuse to help. I have had to be extremely proactive in my own diagnosis, following the path of autoimmune conditions (co-morbid
Due to my ongoing failing health I've had to do my own research as to the pathway of blood test results, symptoms and the progression/knock on effects of having doctors who refuse to help. I have had to be extremely proactive in my own diagnosis, following the path of autoimmune conditions (co-morbid
Allywales8663
in
Pernicious Anaemia Society
7 days ago
Transitioning to Armour Thyroid
Hi everyone, I was diagnosed with an underactive thyroid at 21 and I've also got Hashimoto's. I recently changed from Levo/T3 to Armour, under the guidance of a lovely private endo, and I'm currently on three and a half grains per day, split into two doses. I wondered if anyone else has had side effects
Hi everyone, I was diagnosed with an underactive thyroid at 21 and I've also got Hashimoto's. I recently changed from Levo/T3 to Armour, under the guidance of a lovely private endo, and I'm currently on three and a half grains per day, split into two doses. I wondered if anyone else has had side effects
Jojozo
in
Thyroid UK
7 days ago
Assistant Dogs.
I searched google a few years ago about assistant dogs because I thought I need one of them, but I got nowhere. Today I saw a demonstration of an assistant dog at work, it brought me to tears because it showed me just how much I do need one, how good , helpful it would be. I really think it would
I searched google a few years ago about assistant dogs because I thought I need one of them, but I got nowhere. Today I saw a demonstration of an assistant dog at work, it brought me to tears because it showed me just how much I do need one, how good , helpful it would be. I really think it would
saxcat
in
Fibromyalgia Action UK
7 days ago
RA and rashes
hi, I’m just wondering if you can get rashes with RA.. I’ve developed a few patches of small rashes possibly a bit like hives, though one is a circular rash (which aware could be ringworm but don’t think it is).. also aware these may just be fungal rashes. we have lupus in the family and although
hi, I’m just wondering if you can get rashes with RA.. I’ve developed a few patches of small rashes possibly a bit like hives, though one is a circular rash (which aware could be ringworm but don’t think it is).. also aware these may just be fungal rashes. we have lupus in the family and although
Sapphire1701
in
NRAS
8 days ago
Lupus connected to Radiation
I recently read an article where someone felt that Lupus was connected to radiation exposure. Around 1989 I had a full radiation treatment for breast cancer. Back then they radiated your entire side back to front and I had horrific burns. 25 years later I was diagnosed with Sjogrens and Lupus. Has anyone
I recently read an article where someone felt that Lupus was connected to radiation exposure. Around 1989 I had a full radiation treatment for breast cancer. Back then they radiated your entire side back to front and I had horrific burns. 25 years later I was diagnosed with Sjogrens and Lupus. Has anyone
DogHospiceMom
in
LUPUS UK
8 days ago
Patient's view least important in diagnosis 🙄
Who'd have thought it? Research for Lupus Trust and in a Sjogren's UK newsletter but very applicable for us and others...https://academic.oup.com/rheumatology/advance-article/doi/10.1093/rheumatology/kead685/7473364?login=false UPDATE: larger photos of all three pages of the article uploaded below.
Who'd have thought it? Research for Lupus Trust and in a Sjogren's UK newsletter but very applicable for us and others...https://academic.oup.com/rheumatology/advance-article/doi/10.1093/rheumatology/kead685/7473364?login=false UPDATE: larger photos of all three pages of the article uploaded below.
Agitator23
in
Thyroid UK
8 days ago
After 25 years they have stopped my B12 - what can I do?
I'm in my early sixties. Generally very good health. On no medication. About twenty five years ago my then brilliant GP did a blood test for B12. A few days later rang me to come to the surgery immediately where he injected B12 himself. Apparently I had dangerously low levels of B12 that indicated I
I'm in my early sixties. Generally very good health. On no medication. About twenty five years ago my then brilliant GP did a blood test for B12. A few days later rang me to come to the surgery immediately where he injected B12 himself. Apparently I had dangerously low levels of B12 that indicated I
DIYenthusiast
in
Pernicious Anaemia Society
8 days ago
overactive to underactive
Hi Everyone, I’m a newbie to all this but i certainly need some advice as i feel like im in the dark with my doctors and endocrinologists i don’t exactly know anything apart from having an overactive thyroid which was treated for 18months then went into remission but came back 8months later then thyroid
Hi Everyone, I’m a newbie to all this but i certainly need some advice as i feel like im in the dark with my doctors and endocrinologists i don’t exactly know anything apart from having an overactive thyroid which was treated for 18months then went into remission but came back 8months later then thyroid
Leeleemarksy86
in
Thyroid UK
9 days ago
has anyone got Lupus in their eyes?
I have been told I have Lupus in my eyes. Does anyone else have this? Thank you
I have been told I have Lupus in my eyes. Does anyone else have this? Thank you
drobbie
in
LUPUS UK
9 days ago
PBC & Lupus
Hi, I'm just wondering if anyone here has Lupus along with PBC? I have developed a distinct butterfly rash on my face that has been appearing on and off over the last few weeks. In late 2022 I became aware that a blood pressure med I was taking seemed to be causing a rash. If I stopped it, the rash went
Hi, I'm just wondering if anyone here has Lupus along with PBC? I have developed a distinct butterfly rash on my face that has been appearing on and off over the last few weeks. In late 2022 I became aware that a blood pressure med I was taking seemed to be causing a rash. If I stopped it, the rash went
Turquoise2075
in
PBC Foundation
10 days ago
Sle lupus
Hi I have sle lupus , my skin is itching 24/7, plus dreadful spasms of pain any tips? , also awaiting to see a new rhematologist for some treatment.
Hi I have sle lupus , my skin is itching 24/7, plus dreadful spasms of pain any tips? , also awaiting to see a new rhematologist for some treatment.
Sunflower1921
in
NRAS
11 days ago
are atrophic gastritis and pernicious anemia the same thing
hello all, I was wondering if the atrophic gastritis and PA are the same thing.
hello all, I was wondering if the atrophic gastritis and PA are the same thing.
JesusMercy60
in
Pernicious Anaemia Society
11 days ago
Bupa Doctor Recommendations for Hashimotos, Hypothyroidism and Pernicious Anaemia
Hi! I'm looking for recommendations for specialists in these areas: Hashimotos Hypothyroidism Pernicious Anaemia The recommendations are for my wife who has Bupa private healthcare so if anyone has recommendations for bupa that would be great, however, I'd be happy to hear other private doctors
Hi! I'm looking for recommendations for specialists in these areas: Hashimotos Hypothyroidism Pernicious Anaemia The recommendations are for my wife who has Bupa private healthcare so if anyone has recommendations for bupa that would be great, however, I'd be happy to hear other private doctors
mxnero
in
Thyroid UK
11 days ago
Self-Management Tips
Hello to our lovely Health Unlocked Community! We’re excited to share some helpful tips on self-managing arthritis to empower you in making informed decisions about your health and wellbeing. Self-management means taking control of your condition by using techniques that work best for you to manage
Hello to our lovely Health Unlocked Community! We’re excited to share some helpful tips on self-managing arthritis to empower you in making informed decisions about your health and wellbeing. Self-management means taking control of your condition by using techniques that work best for you to manage
arthritis_action
Partner
in
Arthritis Action
12 days ago
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